Smith & Nephew recalls OSTEORAPTOR 2.9 absorbable suture anchors with specific batch numbers due to potential sterile packaging breaches that could compromise surgical safety.
Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
Smith & Nephew is recalling certain OSTEORAPTOR 2.9 absorbable suture anchors because the packaging might not seal properly, risking contamination during surgery. This could lead to infections or other complications if the sterile barrier is broken.
The packaging may not seal correctly, which could allow contaminants to enter the sterile product. This might compromise the surgical site and increase infection risk during procedures.
Surgical patients and medical professionals who use the recalled OSTEORAPTOR 2.9 suture anchors. Those most at risk are individuals undergoing surgery with these specific products.
Check for the product name 'OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE' and batch numbers listed in the recall (e.g., 2012909, 2012911, etc.). The product number is 72201995.
Identify the product number (72201995) and batch numbers listed in the recall to confirm if your item is affected.
The recall indicates a potential risk of packaging breach, but the product is not unsafe if the packaging seals properly. Affected units should be checked and handled according to the recall instructions.
The recall does not specify a remedy, so contact Smith & Nephew directly to determine if your specific batch number is affected and what steps to take.
Look for the product number 72201995 and batch numbers listed in the recall (e.g., 2012909, 2012911, etc.) on the packaging.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0152-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0152-2021 from Smith & Nephew. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
